A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand

Brugada综合征 增强子 基因座(遗传学) 遗传学 生物 等位基因 全基因组关联研究 心源性猝死 钠通道 基因 医学 单核苷酸多态性 转录因子 基因型 内科学 神经科学 化学 有机化学
作者
Roddy Walsh,John Mauleekoonphairoj,Isabella Mengarelli,Fernanda M. Bosada,Arie O. Verkerk,Karel van Duijvenboden,Yong Poovorawan,Wanwarang Wongcharoen,Boosamas Sutjaporn,Pharawee Wandee,Nitinan Chimparlee,Ronpichai Chokesuwattanaskul,Kornkiat Vongpaisarnsin,Piyawan Dangkao,Cheng‐I Wu,Rafik Tadros,Ahmad S. Amin,Krystien V.V. Lieve,Pieter G. Postema,Maarten Kooyman,Leander Beekman,Dujdao Sahasatas,Montawatt Amnueypol,Rungroj Krittayaphong,Somchai Prechawat,Alisara Anannab,Pattarapong Makarawate,Tachapong Ngarmukos,Keerapa Phusanti,Gumpanart Veerakul,Zoya Kingsbury,Taksina Newington,Uma Maheswari,Mark T. Ross,Andrew A. Grace,Pier D. Lambiase,Elijah R. Behr,Jean‐Jacques Schott,Richard Redon,Julien Barc,Vincent M. Christoffels,Arthur A.M. Wilde,Koonlawee Nademanee,Connie R. Bezzina,Apichai Khongphatthanayothin
出处
期刊:Circulation [Ovid Technologies (Wolters Kluwer)]
标识
DOI:10.1161/circulationaha.124.069041
摘要

BACKGROUND: Brugada syndrome (BrS) is a cardiac arrhythmia disorder that causes sudden death in young adults. Rare genetic variants in the SCN5A gene encoding the Na v 1.5 sodium channel and common noncoding variants at this locus are robustly associated with the condition. BrS is particularly prevalent in Southeast Asia but the underlying ancestry-specific factors remain largely unknown. METHODS: Genome sequencing of BrS probands and population-matched controls from Thailand was performed to identify rare noncoding variants at the SCN5A-SCN10A locus that were enriched in patients with BrS. A likely causal variant was prioritized by computational methods and introduced into human induced pluripotent stem cell (hiPSC) lines using CRISPR-Cas9. The effect of the variant on SCN5A expression and Na v 1.5 sodium channel current was then assessed in hiPSC-derived cardiomyocytes (hiPSC-CMs). RESULTS: A rare noncoding variant in an SCN5A intronic enhancer region was highly enriched in patients with BrS (detected in 3.9% of cases with a case-control odds ratio of 45.2). The variant affects a nucleotide conserved across all mammalian species and predicted to disrupt a Mef2 transcription factor binding site. Heterozygous introduction of the enhancer variant in hiPSC-CMs caused significantly reduced SCN5A expression from the variant-containing allele and a 30% reduction in Na v 1.5-mediated sodium current density compared with isogenic controls, confirming its pathogenicity. Patients with the variant had severe phenotypes, with 89% experiencing cardiac arrest. CONCLUSIONS: This is the first example of a functionally validated rare noncoding variant at the SCN5A locus and highlights how genome sequencing in understudied populations can identify novel disease mechanisms. The variant partly explains the increased prevalence of BrS in this region and enables the identification of at-risk variant carriers to reduce the burden of sudden cardiac death in Thailand.
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